K-number	K890709
Device name	O.R. TOWELS (STERILE)
Applicant	Cypress Medical Products, Ltd.
Product code	KKX
Device class	Class II
Decision date	Mar 14, 1989
Decision	Substantially Equivalent
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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O.R. TOWELS (STERILE)

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